Suchergebnisse - "Copeland, William"

PubPharm (17)

1

Single-molecule level structural dynamics of DNA unwinding by human mitochondrial Twinkle helicase

enthalten in: The Journal of biological chemistry | 2020

von Kaur, P. | Longley, M. | Pan, H. | +4

2

Complementation of aprataxin deficiency by base excision repair enzymes in mitochondrial extracts

enthalten in: Nucleic acids research | 2017

von Çaglayan, M. | Prasad, R. | Krasich, R. | +8

3

DNA polymerase θ specializes in incorporating synthetic expanded-size (xDNA) nucleotides

enthalten in: Nucleic acids research | 2016

von Kent, T. | Rusanov, T. | Hoang, T. | +5

4

POLG2 disease variants : analyses reveal a dominant negative heterodimer, altered mitochondrial localization and impaired respiratory capacity

enthalten in: Human molecular genetics | 2015

von Young, M. | Humble, M. | DeBalsi, K. | +2

5

High quality methylome-wide investigations through next-generation sequencing of DNA from a single archived dry blood spot

enthalten in: Epigenetics | 2013

von Aberg, K. | Xie, L. | Nerella, S. | +3

6

Biochemical analysis of the G517V POLG variant reveals wild-type like activity

enthalten in: Mitochondrion | 2011

von Kasiviswanathan, R. | Copeland, W.

7

Disease variants of the human mitochondrial DNA helicase encoded by C10orf2 differentially alter protein stability, nucleotide hydrolysis, and helicase activity

enthalten in: The Journal of biological chemistry | 2010

von Longley, M. | Humble, M. | Sharief, F. | +1

8

Preparation of human mitochondrial single-stranded DNA-binding protein

enthalten in: Methods in molecular biology (Clifton, N.J.) | 2009

von Longley, M. | Smith, L. | Copeland, W.

9

The DNA polymerase gamma Y955C disease variant associated with PEO and parkinsonism mediates the incorporation and translesion synthesis opposite 7,8-dihydro-8-oxo-2'-deoxyguanosine

enthalten in: Human molecular genetics | 2007

von Graziewicz, M. | Bienstock, R. | Copeland, W.

10

Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders

enthalten in: Human molecular genetics | 2006

von Chan, S. | Longley, M. | Copeland, W.